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  2. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is the organic compound with the formula C 6 H 5 C(O)CH 3. It is the simplest aromatic ketone . This colorless, viscous liquid is a precursor to useful resins and fragrances.

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    [4] To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively ...

  4. Acetanisole - Wikipedia

    en.wikipedia.org/wiki/Acetanisole

    Its chemical names are based on considering the structure as either an acetyl (methyl-ketone) analog of anisole. Other names It can also be seen as a methyl ether analog of acetophenone . Acetanisole is found naturally in castoreum , the glandular secretion of the beaver .

  5. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Like most ketones, acetone exhibits the keto–enol tautomerism in which the nominal keto structure (CH 3) 2 C=O of acetone itself is in equilibrium with the enol isomer (CH 3)C(OH)=(CH 2) (prop-1-en-2-ol). In acetone vapor at ambient temperature, only 2.4 × 10 −7 % of the molecules are in the enol form. [46]

  6. Naproxen - Wikipedia

    en.wikipedia.org/wiki/Naproxen

    OTC preparations of naproxen in the U.S. are mainly marketed by Bayer HealthCare under the brand name Aleve and generic store brand formulations in 220 mg tablets. [44] In Australia, packets of 275 mg tablets of naproxen sodium are Schedule 2 pharmacy medicines , with a maximum daily dose of five tablets or 1375 mg.

  7. Phenacyl bromide - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_bromide

    Phenacyl bromide is the organic compound with the formula C 6 H 5 C(O)CH 2 Br. This colourless solid is a powerful lachrymator as well as a useful precursor to other organic compounds. It is prepared by bromination of acetophenone: [2] C 6 H 5 C(O)CH 3 + Br 2 → C 6 H 5 C(O)CH 2 Br + HBr. The compound was first reported in 1871. [3]

  8. Phenacyl chloride - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_chloride

    Phenacyl chloride, also commonly known as chloroacetophenone, is a substituted acetophenone.It is a useful building block in organic chemistry.Apart from that, it has been historically used as a riot control agent, where it is designated CN. [5]

  9. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

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